rs2227589, SERPINC1

N. diseases: 3
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 0.925 0.120 1 173917078 intron variant C/T snv 9.6E-02 0.030 1.000 3 2013 2019
Antithrombin III Deficiency
CUI: C0272375
Disease: Antithrombin III Deficiency
52 0.925 0.120 1 173917078 intron variant C/T snv 9.6E-02 0.010 1.000 1 2019 2019
Deep Vein Thrombosis
CUI: C0149871
Disease: Deep Vein Thrombosis
93 0.925 0.120 1 173917078 intron variant C/T snv 9.6E-02 0.010 1.000 1 2008 2008